In vitro effects of cadmium and mercury on Pacific oyster, Crassostrea gigas (Thunberg), haemocytes

• Published in: Fish & shellfish immunology Vol. 16; no. 4; pp. 501 - 512
• Main Authors: Gagnaire, B, Thomas-Guyon, H, Renault, T
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.04.2004
• Subjects: Aminopeptidases - metabolism; Animals; Cadmium; Cadmium - toxicity; Cell Survival - drug effects; Cellular activities; Crassostrea gigas; Dose-Response Relationship, Drug; Esterases - metabolism; Flow Cytometry; Haemocytes; Hemocytes - drug effects; Hemocytes - metabolism; In Vitro Techniques; Mercury; Mercury - toxicity; Monophenol Monooxygenase - metabolism; Ostreidae - enzymology; Ostreidae - metabolism; Peroxidase - metabolism; Phagocytosis - drug effects; Phenoloxidase; Toxicity; Toxicity Tests, Acute; Water Pollutants, Chemical - toxicity; Phenoloxidase; Flow cytometry; Cadmium; Toxicity; Haemocytes; Cellular activities; Mercury; Crassostrea gigas
• ISSN: 1050-4648; 1095-9947
• DOI: 10.1016/j.fsi.2003.08.007

In the past decades, shellfish culture has developed in a significant way around the world. However, culture areas are often subject to recurring anthropic pollution. The recrudescent presence of industrial wastes is a source of heavy metals and results in pollutant transfer towards the aquatic environment in estuarine areas. Because of their mode of life, bivalves, including mussels and oysters, are suggested as ideal indicator organisms. The development of techniques allowing the analysis of the effects of pollutants on bivalve biology may lead to the monitoring of pollutant transfer in estuarine areas. In this context, the effects of cadmium and mercury on defence mechanisms were analysed in Pacific oysters, Crassostrea gigas. Pollutant effects were tested in vitro on oyster haemocytes. Cell viability and enzymatic activities (esterase, peroxidase, aminopeptidase, phagocytosis activities) were monitored by flow cytometry. Enzymatic phenoloxidase-like activity was also evaluated by spectrophotometry. High pollutant concentrations were used in order to detect the acute effect and to approach real pollutant concentrations existing in animal tissues. Cadmium induced no effect on oyster haemocytes under the tested conditions. On the contrary, mercury caused a significant haemocyte mortality after a 24 h in vitro incubation. Aminopeptidase positive cell percentage was enhanced by the pollutant, and phenoloxidase-like activity was inhibited. These in vitro results show that mercury may be expected to have an impact on bivalve immune functions in contaminated areas.